Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Thiocarbohydrazide | HCID 2724189 | — |
| Reactant | Ketomalonic acid hydrate | HCID 20057180 | — |
| Reactant | HCID 178514284 | HCID 178514284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178475129 | HCID 178475129 | — |
Reaction Steps
Example 1 is repeated using 1.0 g of 6-carboxy-3-mercapto-4-amino-1,2,4-triazin-5-one, prepared from ketomalonic acid hydrate and thiocarbohydrazide as previously described in my application Ser. No. 6/238,480 (filed 2/26/81), in 30 ml of acetic anhydride. The reaction mixture is heated at 80° C. to dissolve the acid; then for one hour at 90° C. and then for 3 hours at 110° C. The product, isolated as before, melts at 50°-60° C. and is soluble in acetone and alcohol. It decomposes at about 120° C. Anal. Calcd. for C10H14O4N4S: S, 11.29. Found: S, 11.29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405779 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-18ec7df48fa14bab99f3f64e1ea70ebd |
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| Source note | uspto-grants-1983_09 |
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